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Located at 275-39 St Kilda Road in Melbourne's 3004 postcode, The Public Land Consultancy provides independent professional advice for managers and users of public land. Their services encompass consultancy, professional development, and various training courses aimed at enhancing the management and governance of public land in Victoria. The consultancy works with a range of clients, including government bodies and local councils, addressing issues such as access to land for renewable energy projects, governance of recreational facilities, and strategies for managing community use of public spaces. Through their expertise, they aim to improve the planning, management, and development of public land across the region. Generated from the website

The Public Land Consultancy, located in Melbourne, provides independent professional advice for managers and users of public land, addressing various issues from coastal erosion to governance of recreational boating facilities. They offer a range of consultancy services, professional development courses, and research on public land management in Victoria. With experience spanning numerous projects, including community facilities and sustainability initiatives, the consultancy collaborates with various government bodies and organizations to ensure effective management and utilization of public land. Their expertise covers areas such as land planning, legislation, and community strategies, contributing to the livability of Melbourne and its surrounding regions. Generated from the website

The Aplastic Anaemia and Other Bone Marrow Failure Syndromes Registry (AAR) in Melbourne is a clinical quality registry that gathers health information on patients diagnosed with aplastic anaemia and inherited bone marrow failure syndromes across Australia. Managed by Monash University's School of Public Health and Preventive Medicine, the registry aims to enhance patient care and outcomes through comprehensive data collection regarding diagnosis, treatment, and quality of life. Participating in the AAR allows patients to contribute valuable data that combines to form a clearer understanding of these rare conditions, ultimately benefiting all patients involved. The registry is supported by various initiatives, including funding from Maddie Riewoldt's Vision, reflecting a commitment to advancing research and treatment in this field. Generated from the website